meddevicedb.com FDA Device Reference

Snap-Off Self-Compressive Screw

K150772 Class II Traditional
Decision Date
2015-05-08
Sponsor / Applicant
Neosteo

Technical Specification

510(k) Submission ID K150772
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2015-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Snap-Off Self-Compressive Screw received FDA 510(k) clearance under submission number K150772, sponsored by Neosteo. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.